Phenotype #0000302295

Individual ID 00410191
Associated disease -
Phenotype details 12y (first visit): best corrected Snellen visual acuity right, left eye: 20/40, 20/40; electroretinograms: full field cone ERG amplitude in microvolts to 30HZ white light (lower norm = 50 microvolts): 0.1 / 0.1; visual field right, left eye: Goldmann total field area to V-4e white test light: 78 / 78; dark adaptation: final threshold in log units above normal after 45 minutes of adaptation: 3; lens right / left eye: central posterior subcapsular cataract / central posterior subcapsular cataract; macula right / left eye: normal / normal; periphery: bone spicule or clumped pigment in one or more quadrants; 30y (last visit): best corrected Snellen visual acuity right, left eye: 20/30, 20/30; electroretinograms: full field cone ERG amplitude in microvolts to 30HZ white light (lower norm = 50 microvolts): not available / not available; visual field right, left eye: Goldmann total field area to V-4e white test light: 43 / 73; dark adaptation: final threshold in log units above normal after 45 minutes of adaptation: not available; lens right / left eye: central posterior subcapsular cataract / central posterior subcapsular cataract; macula right / left eye: normal / normal; periphery: bone spicule or clumped pigment in one or more quadrants
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite retinitis pigmentosa
Age/Examination 30y (30 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2022-05-20 12:01:22 +02:00 (CEST)
Date last edited N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.